A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999124



Internal ID19158660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176805162..176842733hg38UCSC Ensembl
Innerchr3:176522950..176560521hg19UCSC Ensembl
Innerchr3:178005644..178043215hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3837572
hg1937572
hg1837572
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4994n100
Supporting Variantsnssv3614956
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999124
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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